1. |
- Calard, Francois, et al.
(författare)
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Designing sterically demanding thiolate coated AuNPs for electrical characterization of BPDT in a NP-molecule-nanoelectrode platform
- 2017
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Ingår i: Molecular Systems Design & Engineering. - : ROYAL SOC CHEMISTRY. - 2058-9689. ; 2:2, s. 133-139
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Tidskriftsartikel (refereegranskat)abstract
- Molecular electronics with single or few molecules requires a stable metal-molecule nanojunction platform. Herein, we report the design and synthesis of gold nanoparticles coated with sterically demanding thiol ligands that are essential to fabricate a versatile and stable nanoelectrode-molecule-nanoparticle platform suitable for electrical characterization of small organic molecules. By combining.-tetraphenylmethane ether functionalized alkyl thioacetate and alkyl thiols, we prepared highly stable gold nanoparticles in a one-phase reaction providing simple and efficient purification. This robust preparation gives highly pure nanoparticles in very high yields (up to 90%) with long-time shelf stability. The synthesis in this work has superior reproducibility compared to previous synthesis processes that are currently being used for such molecular electronics platforms. Electron microscopy confirms the formation of uniform and small nanoparticles in the range of 5 to 7 nm. These nanoparticles with different ligand surface coverages were placed in a 20 nm nanoelectrode setup using dielectrophoretic forces. This setup was utilized to characterize the conductivity of the molecular wire 4,4'-biphenyldithiol introduced via ligand placeexchange under ambient conditions.
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2. |
- Wani, Ishtiaq Hassan, 1985-, et al.
(författare)
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A sub 20 nm metal-conjugated molecule junction acting as a nitrogen dioxide sensor
- 2019
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Ingår i: Nanoscale. - : Royal Society of Chemistry (RSC). - 2040-3364 .- 2040-3372. ; 11:14, s. 6571-6575
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Tidskriftsartikel (refereegranskat)abstract
- The interaction of a gas molecule with a sensing material causes the highest change in the electronic structure of the latter, when this material consists of only a few atoms. If the sensing material consists of a short, conductive molecule, the sensing action can be furthermore probed by connecting such molecules to nanoelectrodes. Here, we report that NO2 molecules that adhere to 4,4'-biphenyldithiol (BPDT) bound to Au surfaces lead to a change of the electrical transmission of the BPDT. The related device shows reproducible, stable measurements and is so far the smallest (<20 nm) gas sensor. It demonstrates modulation of charge transport through molecules upon exposure to nitrogen dioxide down to concentrations of 55 ppb. We have evaluated several devices and exposure conditions and obtained a close to linear dependence of the sensor response on the gas concentration.
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6. |
- Jafri, Syed Hassan Mujtaba, 1979-, et al.
(författare)
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Nanomolecular electronic devices based on AuNP molecule nanoelectrodes using molecular place-exchange process
- 2020
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Ingår i: Nanotechnology. - : IOP PUBLISHING LTD. - 0957-4484 .- 1361-6528. ; 31:22
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Tidskriftsartikel (refereegranskat)abstract
- The implementation of electronics applications based on molecular electronics devices is hampered by the difficulty of placing a single or a few molecules with application-specific electronic properties in between metallic nanocontacts. Here, we present a novel method to fabricate 20 nm sized nanomolecular electronic devices (nanoMoED) using a molecular place-exchange process of nonconductive short alkyl thiolates with various short chain conductive oligomers. After the successful place-exchange with short-chain conjugated oligomers in the nanoMoED devices, a change in device resistance of up to four orders of magnitude for 4,4 '-biphenyldithiol (BPDT), and up to three orders of magnitude for oligo phenylene-ethynylene (OPE), were observed. The place-exchange process in nanoMoEDs are verified by measuring changes in device resistance during repetitive place-exchange processes between conductive and nonconductive molecules and surface-enhanced Raman spectroscopy. This opens vast possibilities for the fabrication and application of nanoMoED devices with a large variety of molecules.
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7. |
- Li, Hu, 1986-, et al.
(författare)
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Enhanced gas sensing performance of graphene/ZnS-CdS hetero-nanowires gas sensor synthesized by Langmuir-Blodgett self-assembly method
- 2017
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Ingår i: Journal of Physics Conference Series. - : IOP Publishing. - 1742-6588 .- 1742-6596. ; 922
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Tidskriftsartikel (refereegranskat)abstract
- Graphene is a promising material in the field of solid-state gas sensors due to the unique two-dimensional structure. Here, we have shown by fabricating graphene/ZnS-CdS hetero-nanowire structure, the gas sensor sensitivity has a two-fold increase to 20% under 15 ppm gaseous concentration compared to a 10% response in pristine graphene. Spectroscopy and microscopy analysis indicate that the semi-conducting ZnS-CdS hetero-nanowires are 2 nm wide and densely packed on top of graphene. By combining UV illumination, the device approaches a fast response/recovery and high gas sensitivity, thus has a potential to be used in a detection of wide range of gases.
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8. |
- Rubino, Stefano, 1978-, et al.
(författare)
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In-situ contacting of nanosheets and remote EMCD
- 2009
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Ingår i: 2nd International Workshop on Remote Electron Microscopy and In Situ Studies, Gothenburg, Sweden 16-18 November 2009.
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Konferensbidrag (övrigt vetenskapligt/konstnärligt)
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9. |
- Sher, Omer, et al.
(författare)
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Analysis of molecular ligand functionalization process in nano-molecular electronic devices containing densely packed nano-particle functionalization shells
- 2022
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Ingår i: Nanotechnology. - : IOP Publishing. - 0957-4484 .- 1361-6528. ; 33:25
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Tidskriftsartikel (refereegranskat)abstract
- Molecular electronic devices based on few and single-molecules have the advantage that the electronic signature of the device is directly dependent on the electronic structure of the molecules as well as of the electrode-molecule junction. In this work, we use a two-step approach to synthesise functionalized nanomolecular electronic devices (nanoMoED). In first step we apply an organic solvent-based gold nanoparticle (AuNP) synthesis method to form either a 1-dodecanethiol or a mixed 1-dodecanethiol/omega-tetraphenyl ether substituted 1-dodecanethiol ligand shell. The functionalization of these AuNPs is tuned in a second step by a ligand functionalization process where biphenyldithiol (BPDT) molecules are introduced as bridging ligands into the shell of the AuNPs. From subsequent structural analysis and electrical measurements, we could observe a successful molecular functionalization in nanoMoED devices as well as we could deduce that differences in electrical properties between two different device types are related to the differences in the molecular functionalization process for the two different AuNPs synthesized in first step. The same devices yielded successful NO2 gas sensing. This opens the pathway for a simplified synthesis/fabrication of molecular electronic devices with application potential.
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10. |
- Ali, Hasan, 1985-, et al.
(författare)
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An electron energy loss spectrometer based streak camera for time resolved TEM measurements
- 2017
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Ingår i: Ultramicroscopy. - : Elsevier BV. - 0304-3991 .- 1879-2723. ; 176, s. 5-10
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Tidskriftsartikel (refereegranskat)abstract
- We propose an experimental setup based on a streak camera approach inside an energy filter to measure time resolved properties of materials in the transmission electron microscope (TEM). In order to put in place the streak camera, a beam sweeper was built inside an energy filter. After exciting the TEM sample, the beam is swept across the CCD camera of the filter. We describe different parts of the setup at the example of a magnetic measurement. This setup is capable to acquire time resolved diffraction patterns, electron energy loss spectra (EELS) and images with total streaking times in the range between 100 ns and 10 μs.
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11. |
- Ghajeri, Farnaz, et al.
(författare)
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Case Study of a Green Nanoporous Material from Synthesis to Commercialisation : Quartzene®
- 2018
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Ingår i: Current Opinion in Green and Sustainable Chemistry. - : Elsevier. - 2452-2236. ; 12, s. 101-109
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Tidskriftsartikel (refereegranskat)abstract
- Synthetic amorphous silicas with high porosity (94–97%) are introduced and various pathways for their synthesis are presented. The materials have structures with high surface area (300–750 m2/g) and are commercialised under the name of Quartzene®. Low cost silica sources and ambient pressure drying enable production in large scale with approximately 70% cost reduction as compared to conventional method silica aerogels. The structure is analysed, properties are reported as low density (0.04–0.15 g/ml), low thermal conductivity (24–26 mW/m·K), etc. Formaldehyde gas adsorption tests reveal that the uptake level of samples made by Quartzene® is significantly increased as compared to commercially available adsorbents. Thermal conductivity at elevated temperatures for mixtures of Quartzene® and stone wool shows a 23% reduction at 650 °C as compared to pure stone wool. Scaling up process for this green material meeting environmental sustainability demands in industrial manufacturing is discussed and challenges/current developments are presented.
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12. |
- Grigoriev, Anton, et al.
(författare)
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Comment on "Quantum interference effects in biphenyl dithiol for gas detection" by J. Prasongkit and A. R. Rocha, RSC Adv., 2016, 64, 59299-59304
- 2020
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Ingår i: RSC Advances. - : Royal Society of Chemistry (RSC). - 2046-2069. ; 10:4, s. 2073-2074
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Tidskriftsartikel (övrigt vetenskapligt/konstnärligt)abstract
- The paper [Prasongkit et al., RSC Adv., 2016, 64, 59299] by Prasongkit and Rocha calculates the binding energy of gas molecules attached to 1-8-biphenyl-dithiol (BPDT) molecules. We find from our calculations, that the binding energies calculated for the NO2 molecules are too low, most likely due to lacking optimization of the site at which the gas molecule binds to the BPDT. Though not shown explicitly here, the same statement might apply to the other gas molecules used in this paper.
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13. |
- Han, Yuanyuan, et al.
(författare)
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Graphene Based Mechanical Biosensor by Employing Non-covalent Stacking Functionalization
- 2019
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Annan publikation (övrigt vetenskapligt/konstnärligt)abstract
- Herein we demonstrate a novel methodology to achieve mechanical biosensor by employing the distinguished interaction forces between the atomic force microscope (AFM) probe and sensor surfaces as the response signal. This mechanical biosensor is fabricated by utilizing the non-covalent π-π stacking of pyrene-maltose onto graphene surfaces with Concanavalin A (Con A) as a target protein. The atomic resolution scanning tunneling microscopy (STM) images indicate the successful formation of the self-assembled and densely packed pyrene-maltose layer on the sensor surface, which gives distinct atomic lattice structure as compared to pristine graphene. This mechanical biosensor exhibits detection of Con A with the sensitivity down to nanomolar level. Therefore, this proposed mechanical biosensor has the potential to be employed in a variety of bio-sensing applications.
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14. |
- Han, Yuanyuan, et al.
(författare)
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Optimization and analysis of pyrene-maltose functionalized graphene surfaces for Con A detection
- 2020
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Ingår i: Applied Surface Science. - : ELSEVIER. - 0169-4332 .- 1873-5584. ; 510
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Tidskriftsartikel (refereegranskat)abstract
- Utilizing the non-covalent pi-pi stacking of pyrene functionalized molecules onto graphene surfaces has achieved great success in the detection of various bio-objects, while the fundamental investigations on surface modifications stills remain rarely exploited. Here, we report the nano and atomic scale analysis of the pi-pi stacking functionalized graphene surface regarding to its surface topography, molecular self-assembly as well as process optimizations. The 'amphipathic' molecule, pyrene-maltose, is used for the non-covalent functionalization of graphene and systematical analysis is performed to understand the influence of different solvents on the molecular surface arrangement. Atomic force microscopy (AFM) and spectroscopy analysis indicate the successful formation of pyrene-maltose layer on graphene surface and it is further confirmed by scanning tunneling microscopy, depicting the self-assembled and densely packed pyrene-maltose layer that give distinguished and ordered diamond-shape lattice as compared to triangular lattice in pristine graphene. We also demonstrated that the interfacial adhesion forces between the AFM probe and the functionalized surfaces allow the detection of the lectin protein Concavalin A through selective absorption. This work provides essential evidence of the pi-pi interactions between pyrene molecules and graphene, and the AFM based adhesion measurement also has the potential to be employed in a variety of bio-detection applications.
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15. |
- Jafri, Syed Hassan Mujtaba, 1979-
(författare)
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Building Systems for Electronic Probing of Single Low Dimensional Nano-objects : Application to Molecular Electronics and Defect Induced Graphene
- 2011
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Doktorsavhandling (övrigt vetenskapligt/konstnärligt)abstract
- Nano-objects have unique properties due to their sizes, shapes and structure. When electronic properties of such nano-objects are used to build devices, the control of interfaces at atomic level is required. In this thesis, systems were built that can not only electrically characterize nano-objects, but also allow to analyze a large number of individual nano-objects statistically at the example of graphene and nanoparticle-molecule-nanoelectrode junctions. An in-situ electrical characterization system was developed for the analysis of free standing graphene sheets containing defects created by an acid treatment. The electrical characterization of several hundred sheets revealed that the resistance in acid treated graphene sheets decreased by 50 times as compared to pristine graphene and is explained by the presence of di-vacancy defects. However, the mechanism of defect insertion into graphene is different when graphene is bombarded with a focused ion beam and in this case, the resistance of graphene increases upon defect insertion. The defect insertion becomes even stronger at liquid N2 temperature. A molecular electronics platform with excellent junction properties was fabricated where nanoparticle-molecule chains bridge 15-30nm nanoelectrodes. This approach enabled a systematic evaluation of junctions that were assembled by functionalizing electrode surfaces with alkanethiols and biphenyldithiol. The variations in the molecular device resistance were several orders of magnitude and explained by variations in attachment geometries of molecules. The spread of resistance values of different devices was drastically reduced by using a new functionalization technique that relies on coating of gold nanoparticles with trityl protected alkanedithiols, where the trityl group was removed after trapping of nanoparticles in the electrode gap. This establishment of a reproducible molecular electronics platform enabled the observation of vibrations of a few molecules by inelastic tunneling spectroscopy. Thus this system can be used extensively to characterize molecules as well as build devices based on molecules and nanoparticles.
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16. |
- Li, Hu, 1986-, et al.
(författare)
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Direct writing of lateral fluorographene nanopatterns with tunable bandgaps and its application in new generation of moire superlattice
- 2020
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Ingår i: Applied Physics Reviews. - : American Institute of Physics. - 1931-9401. ; 7:1
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Tidskriftsartikel (refereegranskat)abstract
- One of the primary goals for monolayer device fabrications and an ideal model of graphene as an atomic thin "canvas" is one that permits semiconducting/insulating lateral nanopatterns to be freely and directly drawn on the semimetallic graphene surface. This work demonstrates a reversible electron-beam-activated technique that allows direct writing of semiconducting/insulating fluorographene lateral nanopatterns with tunable bandgaps on the graphene surface with a resolution down to 9-15 nm. This approach overcomes the conventional limit of semiconducting C4F in the single-sided fluorination of supported graphene and achieves insulating C2F. Moreover, applying this technique on bilayer graphene demonstrates for the first time a new type of rectangular moire pattern arising from the generated C2F boat/graphene superlattice. This novel technique constitutes a new approach to fabricating graphene-based flexible and transparent electronic nanodevices with the CxF channels utilized as semiconducting or insulating counterparts, and also opens a route toward the tailoring and engineering of electronic properties of such materials in addition to the dominating triangular moire patterns from a graphene/hBN system.
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17. |
- Li, Hu, 1986-, et al.
(författare)
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Observation of defect density dependent elastic modulus of graphene
- 2023
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Ingår i: Applied Physics Letters. - 0003-6951 .- 1077-3118. ; 123:5
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Tidskriftsartikel (refereegranskat)abstract
- The recent decade has witnessed a tremendous development of graphene applications in many fields; however, as one of the key considerations, the mechanical properties of graphene still remain largely unexplored. Herein, by employing focused ion beam irradiation, graphene with various defect levels is obtained and further investigated by using Raman spectroscopy and scanning tunneling microscopy. Specially, our atomic force microscopy based nanomechanical property measurement demonstrates a clear defect density dependent behavior in the elastic modulus of graphene on a substrate as the defect density is higher than a threshold value of 1012 cm−2, where a clear decay is observed in the stiffness of graphene. This defect density dependence is mainly attributed to the appearance of amorphous graphene, which is further confirmed with our molecular dynamics calculations. Therefore, our reported result provides an essential guidance to enable the rational design of graphene materials in nanodevices, especially from the perspective of mechanical properties.
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18. |
- Li, Hu, 1986-, et al.
(författare)
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Superior adhesion of graphene nanoscrolls
- 2018
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Ingår i: Communications Physics. - : Springer Science and Business Media LLC. - 2399-3650. ; 1
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Tidskriftsartikel (refereegranskat)abstract
- An emerging material in the carbon family, a graphene nanoscroll (GNS) is composed of tubularly scrolled monolayer graphene and has shown superlubricity and large current sustainability, surpassing the properties of monolayer graphene itself. Here we report on the superior adhesion of GNS prepared with a high yield synthesis method that allows for mass production of high quality GNSs. Raman spectra indicate that the GNS still maintains the signature of monolayer graphene, implying the lacking of π-stacking between adjacent layers. Importantly, adhesion measurements using atomic force microscopy reveal these GNSs with height range of 120-130 nm show a 2.5-fold stronger adhesion force than pristine graphene. This result potentially indicates that the GNS has higher adhesion than monolayer graphene and even higher than the liquid-solid and hydrogen-bonding enhanced interfaces which are essential types of adhesions involved in the field of physical adhesions and thus, GNS could be a new candidate for super-strong and lightweight devices.
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19. |
- Ye, Xiaoling, et al.
(författare)
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High Performance Self-Powered Photodetectors Based on Graphene Nanoribbons/Al2O3/InGaZnO Heterojunctions
- 2024
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Ingår i: IEEE Photonics Journal. - : Institute of Electrical and Electronics Engineers (IEEE). - 1943-0655. ; 16:3
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Tidskriftsartikel (refereegranskat)abstract
- Self-powered photodetectors which operate without external power sources hold immense promise in future photodetection systems. To achieve high-performance self-powered optoelectronic devices, efficient electron-hole pair separation is critical to generate high photocurrents. In this work, we successfully synthesized semiconducting graphene nanoribbons (GNRs) with a direct bandgap of 1.80 eV and employed them to construct a high-performance GNR/Al2O3/IGZO heterostructure photodetector. The built-in electric field in the heterojunctions enables this photodetector to exhibit remarkable performance, showing a responsivity of up to 68 mA/W, a detectivity of 8.34 x 1010 Jones, and rapid response times of 21/20 ms at zero bias. Furthermore, the photodetector features a wide spectral detection range of 405 to 1550 nm. These results highlight the promising potential of GNR/IGZO p-n heterojunction-based self-powered photodetectors in optoelectronic applications.
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